AR035478A1 - Acido amida-hidroxamico, acido acetilenico, beta-sulfonamido y fosfinico como inhibidores de la tace, uso de los mismos para la manufactura de un medicamento y composicion farmaceutica que los contiene - Google Patents

Acido amida-hidroxamico, acido acetilenico, beta-sulfonamido y fosfinico como inhibidores de la tace, uso de los mismos para la manufactura de un medicamento y composicion farmaceutica que los contiene

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Publication number
AR035478A1
AR035478A1 ARP000100325A ARP000100325A AR035478A1 AR 035478 A1 AR035478 A1 AR 035478A1 AR P000100325 A ARP000100325 A AR P000100325A AR P000100325 A ARP000100325 A AR P000100325A AR 035478 A1 AR035478 A1 AR 035478A1
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AR
Argentina
Prior art keywords
heteroatoms selected
membered
phenyl
alkyl
cycloalkyl
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ARP000100325A
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English (en)
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Wyeth Corp
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Publication of AR035478A1 publication Critical patent/AR035478A1/es

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    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/78Halides of sulfonic acids
    • C07C309/86Halides of sulfonic acids having halosulfonyl groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/87Halides of sulfonic acids having halosulfonyl groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing singly-bound oxygen atoms bound to the carbon skeleton
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    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/50Organo-phosphines
    • C07F9/53Organo-phosphine oxides; Organo-phosphine thioxides
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/02Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
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    • A61P19/00Drugs for skeletal disorders
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    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01Sulfonic acids
    • C07C309/28Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/41Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing singly-bound oxygen atoms bound to the carbon skeleton
    • C07C309/42Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing singly-bound oxygen atoms bound to the carbon skeleton having the sulfo groups bound to carbon atoms of non-condensed six-membered aromatic rings
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    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/22Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
    • C07C311/29Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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    • C07C2601/14The ring being saturated

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Abstract

Acidos de hidroxamida, caracterizada porque comprenden la fórmula (1) en la cual la parte C(=O) NHOH y la parte -NR5- están unidas a carbonos adyacentes; donde: X es SO2 o -P(O)R10; Y es un anillo de heteroarilo con 5-10 miembros, que tiene entre 1-3 heteroátomos seleccionados entre: N, NR9, S y O, fenilo o naftilo; con la condición de que X y Z pueden no estar ligados a átomos adyacentes de Y; Z es O, NH, CH2 o S; R5 es hidrógeno o alquilo C1-6; R6 y R7 cada uno, de un modo, independiente, son hidrógeno o metilo; R8 es hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, un heteroarilo de 5-7 miembros con 1-3 heteroátomos seleccionados entre; N, NR9, S y O, un heterocicloalquilo de 5 a 7 miembros que tiene 1 o 2 heteroátomos seleccionados entre N, NR9, S y O, o fenilo; Rg es hidrógeno, alquilo C1-6, cicloalquilo C3-6, o fenilo; R10 es alquilo C1-6, cicloalquilo C3-6, fenilo, o heteroarilo de 5 a 7 miembros, con 1-3 heteroátomos seleccionados entre N, NR9, S y O; R11 y R12 son, de un modo independiente, hidrógeno, alquilo C1-6, cicloalquilo C3-6, un heteroarilo de 5 a 7 miembros que tiene 1-3 heteroátomos seleccionados entre N, NR9, S y O, un heterocicloalquilo de 5 a 7 miembros con 1 o 2 heteroátomos seleccionados entre N, NR9, S y O, o fenilo y el enlace doble opcional que está representado por la línea de puntos está presente; o R11 y R12, junto con los carbonos a los que están unidos, forman un anillo de alquilo mono- o bicíclico, de 5 a 10 miembros saturado o insaturado, opcionalmente fusionado a un anillo de cicloalquilo de 5 a 7 miembros saturado o insaturado, un heteroarilo de 5 a 7 miembros con 1-3 heteroátomos seleccionados entre N, NR9, S y O, un heterocicloalquilo de 5 a 7 miembros con 1 o 2 heteroátomos seleccionados entre N, NR9, S y O, anillos de fenilo o naftilo; o R11 y R12, junto con los carbonos a Los que están unidos, forman un heterocicloalquilo mono- o bicíclico, de 5 a 10 miembros saturado o insaturado, con 1-2 heteroátomos seleccionados entre N, NR9, S y O, opcionalmente fusionados a un heteroarilo de 5 a 7 miembros mono- o bicíclico con 5 a 7 miembros, de 1 a 3 heteroátomos seleccionados entre N, NR9, S y O, un anillo de cicloalquilo de 5 a 7 miembros, saturado o insaturado o un anillo de fenilo o naftilo; la línea de puntos representa un enlace doble opcional; y n = 0-2, o una sal farmacéuticamente aceptable de los mismos.
ARP000100325A 1999-01-27 2000-01-26 Acido amida-hidroxamico, acido acetilenico, beta-sulfonamido y fosfinico como inhibidores de la tace, uso de los mismos para la manufactura de un medicamento y composicion farmaceutica que los contiene AR035478A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US23908399A 1999-01-27 1999-01-27

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AR035478A1 true AR035478A1 (es) 2004-06-02

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ID=22900530

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ARP000100325A AR035478A1 (es) 1999-01-27 2000-01-26 Acido amida-hidroxamico, acido acetilenico, beta-sulfonamido y fosfinico como inhibidores de la tace, uso de los mismos para la manufactura de un medicamento y composicion farmaceutica que los contiene

Country Status (16)

Country Link
EP (1) EP1147078A1 (es)
JP (1) JP2002535383A (es)
KR (1) KR20010089617A (es)
CN (1) CN1337944A (es)
AR (1) AR035478A1 (es)
AU (1) AU769410B2 (es)
BR (1) BR0007754A (es)
CA (1) CA2356345A1 (es)
CZ (1) CZ20012709A3 (es)
EA (1) EA200100808A1 (es)
HU (1) HUP0200605A3 (es)
IL (1) IL144321A0 (es)
NO (1) NO20013639D0 (es)
NZ (1) NZ512025A (es)
WO (1) WO2000044711A1 (es)
ZA (1) ZA200104508B (es)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2003304456A1 (en) 2002-12-23 2005-03-16 Wyeth Holdings Corporation Acetylenic aryl sulfonate hydroxamic acid tace and matrix metalloproteinase inhibitors
DK1735274T3 (da) * 2004-03-22 2010-03-29 Southern Res Inst Ikke-peptidinhibitorer af matrixmetalloproteinaser
FR2947268B1 (fr) * 2009-06-30 2011-08-26 Galderma Res & Dev Nouveaux composes benzene-sulfonamides, leur procede de synthese et leur utilisation en medecine ainsi qu'en cosmetique
FR2950057B1 (fr) 2009-09-17 2011-08-26 Galderma Res & Dev Nouveaux composes benzene-carboxylamides, leur procede de synthese et leur utilisation en medecine ainsi qu'en cosmetique
CN113194954A (zh) 2018-10-04 2021-07-30 国家医疗保健研究所 用于治疗角皮病的egfr抑制剂

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5514716A (en) * 1994-02-25 1996-05-07 Sterling Winthrop, Inc. Hydroxamic acid and carboxylic acid derivatives, process for their preparation and use thereof
CO5080759A1 (es) * 1996-05-15 2001-09-25 Bayer Corp Biarilacetilenos como inhibidores de la metaloproteasa de matriz
US5977408A (en) * 1996-10-16 1999-11-02 American Cyanamid Company Preparation and use of β-sulfonamido hydroxamic acids as matrix metalloproteinase and TACE inhibitors
IL129147A0 (en) * 1996-10-16 2000-02-17 American Cyanamid Co The preparation and use of ortho-sulfonamide aryl hydroxamic acids as matrix metalloproteinase and tace inhibitors
KR20010030935A (ko) * 1997-10-06 2001-04-16 윌리암 에이취 캘넌, 에곤 이 버그 매트릭스 메탈로프로테이나제 및 종양괴사인자-α 전환효소 억제제로서의 오르토-설폰아미도 바이사이클릭헤테로아릴 하이드록삼산의 제조 및 용도

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ZA200104508B (en) 2002-09-02
BR0007754A (pt) 2001-11-13
AU769410B2 (en) 2004-01-29
EA200100808A1 (ru) 2001-12-24
AU2630600A (en) 2000-08-18
NO20013639L (no) 2001-07-24
CN1337944A (zh) 2002-02-27
HUP0200605A2 (hu) 2002-07-29
CA2356345A1 (en) 2000-08-03
EP1147078A1 (en) 2001-10-24
NZ512025A (en) 2003-08-29
WO2000044711A1 (en) 2000-08-03
NO20013639D0 (no) 2001-07-24
JP2002535383A (ja) 2002-10-22
KR20010089617A (ko) 2001-10-06
HUP0200605A3 (en) 2005-05-30
IL144321A0 (en) 2002-05-23
CZ20012709A3 (cs) 2002-04-17

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